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Considerable clinical research monitoring experience (comparable to 5 years) with a demonstrated high level of expertise in all aspects of clinical monitoring.... - Indeed
Review clinical research literature. Knowledge of the FDA CFRs and Good Clinical Practice Guidelines associated with CRA activities and ability to be self... - Indeed
Monitor assigned clinical trials performed. Minimum 2 years of experience in the field as a CRA or strong experience in oncology as Research Nurse.... - Indeed
Minimum 5 years of clinical research experience. Oversee clinical trials, ensuring progress meets clinical objectives.... - Indeed
Preference will be given to people who have recent experience in Clinical Research. Monitor clinical trial sites.... - Indeed
Job Posting Covance is hiring experienced CRAs / Clinical Research Associates to monitor with our Early Clinical Development (ECD) group.... - Indeed
The contract CRA will be responsible for monitoring clinical studies according to Covance Standard Operating Procedures, ICH and Guidelines.... - Indeed
The Clinical Research Associate (CRA) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good... - Indeed
CRA, Clinical Research Associate, monitor*, site manager. The Clinical Research Associate (CRA) performs and coordinates all aspects of the clinical monitoring... - Indeed
Escalate quality issues to Clinical Project Manager (CPM), Clinical Research Specialist (CRS) and/or line manager.... - Indeed
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